Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/17553
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dc.contributor.authorYurasakpong L.
dc.contributor.authorNantasenamat C.
dc.contributor.authorNobsathian S.
dc.contributor.authorChaithirayanon K.
dc.contributor.authorApisawetakan S.
dc.date.accessioned2022-03-10T13:17:29Z-
dc.date.available2022-03-10T13:17:29Z-
dc.date.issued2021
dc.identifier.issn14203049
dc.identifier.other2-s2.0-85117570002
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/17553-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85117570002&doi=10.3390%2fmolecules26216377&partnerID=40&md5=b726d863583c9e7689085fd413533be0
dc.description.abstractBetulinic acid (BA) is a pentacyclic triterpene usually isolated from botanical sources. Numerous studies have reported the inhibitory effect of BA against human colorectal cancer cells (CRC). However, its effect on the expression of the molecular chaperone HSPA is unclear. The aim of this research is to investigate the anti-cancer activities of BA purified from Piper retrofractum and study its effect on the expression of HSPA in colorectal cancer HCT116 and SW480 cells. The viability of both cancer cells was reduced after they were treated with an increasing dosage of BA. Flow cytometry assay revealed that levels of cell apoptosis significantly increased after incubation with BA in both cancer cells. Pro-apoptotic markers including Bax, cleaved-caspase-3 and cleaved-caspase-9 were increased while anti-apoptotic marker Bcl-2 was decreased after BA treatment. Western blot also showed that the expression of HSPA fluctuated upon BA treatment, whereby HSPA was increased at lower BA concentrations while at higher BA concentrations HSPA expression was decreased. Preliminary molecular docking assay showed that BA can bind to the nucleotide binding domain of the HSP70 at its ADP-bound state of the HSP70. Although further research is needed to comprehend the BA-HSPA interaction, our findings indicate that BA can be considered as potential candidate for the development of new treatment for colorectal cancer. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
dc.languageen
dc.subjectantineoplastic agent
dc.subjectbetulic acid
dc.subjectheat shock protein 70
dc.subjectpentacyclic triterpene
dc.subjectapoptosis
dc.subjectcell proliferation
dc.subjectcell survival
dc.subjectchemistry
dc.subjectcolorectal tumor
dc.subjectconformation
dc.subjectdose response
dc.subjectdrug effect
dc.subjectflow cytometry
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjecthuman
dc.subjectmetabolism
dc.subjectmolecular docking
dc.subjectmolecular dynamics
dc.subjectstructure activity relation
dc.subjecttumor cell line
dc.subjectAntineoplastic Agents, Phytogenic
dc.subjectApoptosis
dc.subjectCell Line, Tumor
dc.subjectCell Proliferation
dc.subjectCell Survival
dc.subjectColorectal Neoplasms
dc.subjectDose-Response Relationship, Drug
dc.subjectFlow Cytometry
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHSP70 Heat-Shock Proteins
dc.subjectHumans
dc.subjectMolecular Conformation
dc.subjectMolecular Docking Simulation
dc.subjectMolecular Dynamics Simulation
dc.subjectPentacyclic Triterpenes
dc.subjectStructure-Activity Relationship
dc.titleBetulinic acid modulates the expression of hspa and activates apoptosis in two cell lines of human colorectal cancer
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationMolecules. Vol 26, No.21 (2021)
dc.identifier.doi10.3390/molecules26216377
Appears in Collections:Scopus 1983-2021

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